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1 quires residues in the amino terminus of the Agouti protein.
2 yproline residues found in the middle of the agouti protein.
3 ses the effect of the endogenous antagonist, agouti protein.
5 me, which results from ectopic expression of agouti protein, a pigmentation factor normally expressed
6 tions regarding the biochemical mechanism of Agouti protein action, and provide evidence of a novel s
8 , but mutations that cause overexpression of agouti protein, an antagonist of the receptor, result in
12 to the Mc1r, and that the similarity between Agouti protein and Agrp includes their binding sites.
13 binding by the carboxyl-terminal portion of Agouti protein and down-regulation of melanocortin recep
16 rize pharmacologic properties of recombinant Agouti protein, and have directly measured its cell-surf
17 by Agrp, which indicates that alpha-MSH and Agouti protein bind in a mutually exclusive way to the M
19 gmentary effects of Agouti, and suggest that Agouti protein can act as an agonist of the Mc1r in a wa
20 ne-scanning mutagenesis was performed on the agouti protein carboxyl terminus to locate residues impo
21 that the electrophoretic mobility of native Agouti protein corresponds to the mature full-length for
23 and carboxyl-terminal fragments of Agrp and Agouti protein in a sensitive bioassay based on pigment
24 hat BMP signaling controls the expression of Agouti protein in the hair follicle and provide evidence
25 (FAS) gene expression; further, recombinant agouti protein increases in cultured adipocytes and thes
26 n dissociation constants for mouse and human agouti protein inhibition of ligand binding to the melan
31 pic hormone, melanocyte stimulating hormone, agouti protein ligands (in rodents), c-Kit, and the endo
32 sistant to the effects of agouti, suggesting agouti protein may not play a role in human pigmentary v
33 el signaling mechanism whereby alpha-MSH and Agouti protein or Agrp function as independent ligands t
34 ides based on the sequence of this loop from Agouti protein or human AGRP are functional antagonists
35 sibly influencing the biogenesis of secreted agouti protein or modulating protein-protein interaction
39 an adipocytes, and we have shown recombinant agouti protein to increase adipocyte intracellular Ca2+(
40 homology to the corresponding region of the agouti protein, which is an MC1R antagonist involved in
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